| Location | Indianapolis, Indiana |
Genovice is seeking an experienced Validation Consultant to support qualification and validation activities for analytical development and laboratory equipment within a regulated pharmaceutical environment.
Key Responsibilities & Qualifications
Execute and/or support equipment qualification activities, including IQ/OQ/PQ.
Develop and review validation protocols, reports, and associated documentation.
Support qualification of analytical and laboratory instrumentation/equipment.
Work closely with Analytical Development, Quality, Engineering, and Validation teams.
Ensure activities are performed in accordance with GMP requirements and applicable regulatory expectations.
Previous validation/qualification experience within pharmaceutical, biotech, or other regulated life sciences environments required.
Strong technical writing and documentation skills.
Experience with analytical development or QC laboratory equipment strongly preferred.